Webinar – How to Ensure EUDAMED Compliance for Legacy Devices | Ackomas
Hoegl Katharina
Florence Trépant
Jean-Philippe Joubert
Key Takeaways from the Webinar
Join our webinars to explore the latest regulatory compliance strategies in the medical device industry. Our experts provide practical solutions and answer your questions live.
Understand the Definition of Legacy Devices
Legacy devices are those certified under previous directives (MDD/IVDD) and placed on the market after MDR/IVDR dates. They benefit from a transition period—but require strict compliance conditions, including EUDAMED registration.
EUDAMED Registration Is Mandatory
By July 2026, all eligible legacy devices must be registered in EUDAMED, unless a corresponding MDR/IVDR device already exists. Failing to act could block market access.
Ackomas Simplifies Compliance
The Ackomas platform enables automated, secure, and traceable registration of legacy devices, transforming a complex process into a strategic advantage.
Act Early to Avoid Resource Bottlenecks
The closer to the deadline, the harder it becomes to access support and system availability. Starting now secures both time and quality.
EUDAMED & GUDID regulatory alerts — delivered to your inbox
Receive concise updates on MDR/IVDR regulatory changes, EUDAMED registration deadlines, and GUDID compliance requirements. Built for RA/QA and regulatory affairs teams. No promotional content — only actionable changes.
🔒 Our Commitment
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Webinar replays & regulatory briefings
Watch recorded sessions on EUDAMED registration, UDI structuring, and data governance
Deadline alerts & regulatory changes
Be notified when EUDAMED deadlines, MDCG guidance, or submission rules change
Compliance guidance for your team
Practical resources to prepare for audits, structure your UDI data, and manage multi-market registration